Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649556Generated: October 30, 2026

Methanol → HCID 20479068, compound

https://huagongshe.com/reaction/1649556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiboronHCID 6328200—
ReactantHCID 86739130HCID 86739130—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20479068HCID 2047906897.7%

Reaction Steps

To a suspension of 2,4-difluoro-3-aminobutanoic acid hydrochloride (2 g, 11.4 mmol) in anhydrous tetrahydrofuran (THF) (60 mL) at 0° C. is added a solution of 1 M diborane in THF (57 mL, 57 mmol). The reaction mixture is slowly allowed to warm up to room temperature and, after stirring for 12 hours, methanol (60 mL) is added. The solvent is evaporated in vacuo, the residue dissolved in 1 N hydrochloric acid (40 mL), and the aqueous layer extracted twice with ether. The aqueous phase is concentrated in vacuo and the residue washed several times with THF to afford 1,3-difluoro-4-hydroxy-2-aminobutane hydrochloride (1.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04418077
Source datasetuspto-grants-1983_11
ORD IDord-0836091fe7d542cfad10fbdd67e12efa
Source noteuspto-grants-1983_11